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Rapp-Hodgkin ectodermal dysplasia.
O'Donnell BP, James WD. O'Donnell BP, et al. J Am Acad Dermatol. 1992 Aug;27(2 Pt 2):323-6. doi: 10.1016/0190-9622(92)70191-h. J Am Acad Dermatol. 1992. PMID: 1517497 Review.
Rapp-Hodgkin syndrome is a rare condition that is characterized by ectodermal dysplasia and palatal abnormalities. We describe a 24-year-old white woman who has Rapp-Hodgkin syndrome that is associated with a chronic palmar keratoderma, w
Rapp-Hodgkin syndrome is a rare condition that is characterized by ectodermal dysplasia and palatal abnormalities. We d
Rapp-Hodgkin syndrome: an ectodermal dysplasia involving the teeth, hair, nails, and palate. Report of a case and review of the literature.
Crawford PJ, Aldred MJ, Clarke A, Tso MS. Crawford PJ, et al. Oral Surg Oral Med Oral Pathol. 1989 Jan;67(1):50-62. doi: 10.1016/0030-4220(89)90302-2. Oral Surg Oral Med Oral Pathol. 1989. PMID: 2643072 Review.
Rapp-Hodgkin syndrome is a rare form of ectodermal dysplasia involving the hair, eyes, sweat glands, nails, teeth, and palate. ...
Rapp-Hodgkin syndrome is a rare form of ectodermal dysplasia involving the hair, eyes, sweat glands, nails, teeth, and
Rapp-Hodgkin and Hay-Wells ectodermal dysplasia syndromes represent a variable spectrum of the same genetic disorder.
Clements SE, Techanukul T, Holden ST, Mellerio JE, Dorkins H, Escande F, McGrath JA. Clements SE, et al. Br J Dermatol. 2010 Sep;163(3):624-9. doi: 10.1111/j.1365-2133.2010.09859.x. Br J Dermatol. 2010. PMID: 20491771 Review.
BACKGROUND: Rapp-Hodgkin syndrome (RHS) and Hay-Wells [also known as ankyloblepharon-ectodermal defects-cleft lip/palate (AEC)] syndrome have been designated as distinct ectodermal dysplasia syndromes despite both disorders having overlapping clinical feature …
BACKGROUND: Rapp-Hodgkin syndrome (RHS) and Hay-Wells [also known as ankyloblepharon-ectodermal defects-cleft lip/palat …
Skin symptoms in four ectodermal dysplasia syndromes including two case reports of Rapp-Hodgkin-Syndrome.
Knaudt B, Volz T, Krug M, Burgdorf W, Röcken M, Berneburg M. Knaudt B, et al. Eur J Dermatol. 2012 Sep-Oct;22(5):605-13. doi: 10.1684/ejd.2012.1787. Eur J Dermatol. 2012. PMID: 22759387 Review.
These syndromes comprise Christ-Siemens-Touraine syndrome; ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome; ankyloblepharon-ectodermal defects-cleft lip/palate syndrome and Rapp-Hodgkin syndrome. A comprehensive overview of the dermatological …
These syndromes comprise Christ-Siemens-Touraine syndrome; ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome; ankyloblepharon …
A new mutation in TP63 is associated with age-related pathology.
Holder-Espinasse M, Martin-Coignard D, Escande F, Manouvrier-Hanu S. Holder-Espinasse M, et al. Eur J Hum Genet. 2007 Nov;15(11):1115-20. doi: 10.1038/sj.ejhg.5201888. Epub 2007 Jul 4. Eur J Hum Genet. 2007. PMID: 17609671 Review.
We report on a family with four affected adult females presenting with Rapp-Hodgkin syndrome (RHS), an autosomal dominant clinical entity that associates anhidrotic ectodermal dysplasia with cleft lip and palate. ...
We report on a family with four affected adult females presenting with Rapp-Hodgkin syndrome (RHS), an autosomal domina …
Ectodermal dysplasias associated with clefting: significance of scalp dermatitis.
Fosko SW, Stenn KS, Bolognia JL. Fosko SW, et al. J Am Acad Dermatol. 1992 Aug;27(2 Pt 1):249-56. doi: 10.1016/0190-9622(92)70179-j. J Am Acad Dermatol. 1992. PMID: 1341424 Free article. Review.
The three most commonly recognized entities are (1) the EEC syndrome (ectodermal dysplasia, ectrodactyly, cleft lip/palate); (2) the Rapp-Hodgkin syndrome with ectodermal dysplasia, cleft lip/palate, and mid facial hypoplasia; and (3) the Hay-Wells or AEC syn …
The three most commonly recognized entities are (1) the EEC syndrome (ectodermal dysplasia, ectrodactyly, cleft lip/palate); (2) the Rapp